Canonical Allele Identifier: CA2336453950
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41411001C= , CM000681.2:g.41411001C= GRCh38
NC_000019.9:g.41916906C= , CM000681.1:g.41916906C= GRCh37
NC_000019.8:g.46608746C= NCBI36
NG_013004.1:g.18213C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.367C= MANE Select ENSP00000269980.2:p.Gln123=
ENST00000269980.6:c.367C= ENSP00000269980.2:p.Gln123=
ENST00000457836.6:c.301C= ENSP00000416000.2:p.Gln101=
ENST00000538423.5:n.493C=
ENST00000540732.3:c.469C= ENSP00000443246.1:p.Gln157=
ENST00000541315.1:c.174C=
ENST00000542943.5:c.288+185C= ENSP00000440345.1:n.288+185C=
ENST00000595085.5:c.367C= ENSP00000471150.2:p.Gln123=
NM_000709.3:c.367C= NP_000700.1:p.Gln123=
NM_001164783.1:c.367C= NP_001158255.1:p.Gln123=
NM_000709.4:c.367C= MANE Select NP_000700.1:p.Gln123=
NM_001164783.2:c.367C= NP_001158255.1:p.Gln123=